Haase Matthias, Schott Matthias, Bornstein Stefan R, Malendowicz Ludwik K, Scherbaum Werner A, Willenberg Holger S
Department of Endocrinology, Diabetes and Rheumatology, University Hospital Duesseldorf, Moorenstr. 5, D-40225 Duesseldorf, Germany.
J Endocrinol. 2007 Feb;192(2):459-65. doi: 10.1677/JOE-06-0083.
CITED2 gene deletion in mice leads to adrenal agenesis. Therefore, we analyzed CITED2, a CBP/p300 interacting transactivator with transforming activity, in the human adrenal gland. In this study, we examined CITED2 expression in human embryonic and adult adrenal glands as well as adrenocortical carcinomas. As ACTH and basic fibroblast growth factor (bFGF) are connected to the physiology and growth of adrenocortical cells we studied the regulation of CITED2 by these factors in the NCI-H295R adrenocortical carcinoma cell line. We found CITED2 expression in the adult adrenal cortex as well in adrenocortical carcinomas. At an early stage of human adrenal organogenesis CITED2 could be located to the definitive zone of the developing adrenal gland using immunohistochemistry. In NCI-H295R cells, stimulation by bFGF led to a dose-dependent increase in CITED2 promotor activity, mRNA and protein expression while ACTH had no significant effect. The stimulatory effect of bFGF could be reduced by blocking mitogen-activated protein kinase activity using the MAPkinase kinase (MEK1)-inhibitor PD98059. CITED2 is expressed in embryonic and adult human adrenal glands as well as in adrenocortical cancer. It is connected to the signaling cascades of bFGF and its expression is modulated by mitogen-activated protein kinases. This suggests a novel role for CITED2 in human adrenal growth and possibly in adrenal tumorigenesis.
小鼠中CITED2基因缺失会导致肾上腺发育不全。因此,我们对人肾上腺中的CITED2进行了分析,CITED2是一种具有转化活性的CBP/p300相互作用反式激活因子。在本研究中,我们检测了CITED2在人胚胎和成人肾上腺以及肾上腺皮质癌中的表达。由于促肾上腺皮质激素(ACTH)和碱性成纤维细胞生长因子(bFGF)与肾上腺皮质细胞的生理功能和生长相关,我们在NCI-H295R肾上腺皮质癌细胞系中研究了这些因子对CITED2的调控作用。我们发现CITED2在成人肾上腺皮质以及肾上腺皮质癌中均有表达。在人类肾上腺器官发生的早期阶段,使用免疫组织化学方法可将CITED2定位到发育中肾上腺的确立区。在NCI-H295R细胞中,bFGF刺激导致CITED2启动子活性、mRNA和蛋白表达呈剂量依赖性增加,而ACTH无显著影响。使用丝裂原活化蛋白激酶激酶(MEK1)抑制剂PD98059阻断丝裂原活化蛋白激酶活性可降低bFGF的刺激作用。CITED2在胚胎和成人肾上腺以及肾上腺皮质癌中均有表达。它与bFGF的信号级联相关,其表达受丝裂原活化蛋白激酶调节。这表明CITED2在人类肾上腺生长以及可能在肾上腺肿瘤发生中具有新的作用。